prof. dr. Fransiska Malfait
- ORCID iD
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0000-0002-5010-0304
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Heterochronic HOXD13 activation due to 2q31.1 microdeletion results in isolated forearm mesomelic dysplasia
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Understanding human linkeropathies : generation of knock-in models to study of the consequences of defective proteoglycan biosynthesis
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Understanding human linkeropathies : study of the phenotypic and molecular consequences of defective biosynthesis of the glycosaminoglycan tetrasaccharide linker region
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Matrisome gene changes in dorsal root ganglia in mouse models of osteoarthritis pain suggest a role for fibroblast-nociceptor communication in chronic pain
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- Journal Article
- A1
- open access
Pathogenic mechanisms in genetically defined Ehlers-Danlos syndromes
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Classic Ehlers-Danlos syndrome
(2024) GeneReviews®. -
- Journal Article
- A1
- open access
Reduced capsaicin-induced mechanical allodynia and neuronal responses in the dorsal root ganglion in the presence of protein tyrosine phosphatase non-receptor type 6 overexpression
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- Conference Paper
- C3
- open access
When the phenotype is more severe than expected : coexistence of X-linked and dominant ichthyosis in an African patient
(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.402-402 -
Impaired muscle parameters in adults with mild to severe types of osteogenesis imperfecta : a cross-sectional study
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- Journal Article
- A1
- open access
Flemish network on rare connective tissue diseases (CTD) : patient pathways in systemic sclerosis : first steps taken